Sensitivity of CD95-mediated apoptosis has been reported to vary durin
g cell cycle progression (FEBS Lett. (1997) 412, 91-93), Here, we repo
rt that three human glioma cell lines with different p53 status (i) un
dergo growth arrest and synchronous cell cycle re-entry after prolonge
d serum deprivation, (ii) do not exhibit cell cycle-related changes in
CD95 expression at the cell surface, and (iii) do not exhibit cell cy
cle-related changes in susceptibility to DC95 ligand-induced apoptosis
, In contrast, cell cycle-specific activity was demonstrated for vario
us cancer chemotherapy drugs, Further, CD95 expression and susceptibil
ity to CD95 ligand-induced apoptosis does not vary during cell cycle p
rogression of Jurkat T cells, HeLa cervical carcinoma and HepG2 hepato
cellular carcinoma cells. These results do not support a role for the
cell cycle phase as an important predictor of vulnerability to CD95-me
diated apoptosis, (C) 1998 Federation of European Biochemical Societie
s.